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JPS6034512B2 - calcareous ramming material - Google Patents
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JPS6034512B2 - calcareous ramming material - Google Patents

calcareous ramming material

Info

Publication number
JPS6034512B2
JPS6034512B2 JP51050235A JP5023576A JPS6034512B2 JP S6034512 B2 JPS6034512 B2 JP S6034512B2 JP 51050235 A JP51050235 A JP 51050235A JP 5023576 A JP5023576 A JP 5023576A JP S6034512 B2 JPS6034512 B2 JP S6034512B2
Authority
JP
Japan
Prior art keywords
calcareous
clinker
ramming material
weight
mixing
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired
Application number
JP51050235A
Other languages
Japanese (ja)
Other versions
JPS52133310A (en
Inventor
邦男 古川
正治 岡本
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Harima Refractories Co Ltd
Original Assignee
Harima Refractories Co Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Harima Refractories Co Ltd filed Critical Harima Refractories Co Ltd
Priority to JP51050235A priority Critical patent/JPS6034512B2/en
Publication of JPS52133310A publication Critical patent/JPS52133310A/en
Publication of JPS6034512B2 publication Critical patent/JPS6034512B2/en
Expired legal-status Critical Current

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  • Compositions Of Oxide Ceramics (AREA)
  • Ceramic Products (AREA)

Description

【発明の詳細な説明】 本発明は、Si02、Fe203及びTj02等の不純
物の少ない高純度石灰質原料を強競して得られる石灰質
クリンカー又は該クリンカーとマグネシアクリンカー、
ドロマイトクリンカー等との一定比率の混合で得られる
配合調整物に非水溶性のバインダーを添加せる石灰費ラ
ミング材に関する。
DETAILED DESCRIPTION OF THE INVENTION The present invention provides a calcareous clinker obtained by competitively using high-purity calcareous raw materials with few impurities such as Si02, Fe203 and Tj02, or a calcareous clinker and a magnesia clinker,
This invention relates to a lime ramming material in which a water-insoluble binder is added to a mixture prepared by mixing with dolomite clinker or the like at a certain ratio.

Ca○(酸化カルシウム)は非常に高い融点(2$7±
270)を有するので耐火材に使用して効果があり、特
に高温下で蒸気圧が低い等安定しているから高温減圧下
で介在物の少ない清浄な金属を溶製するには好適な耐火
材である。
Ca○ (calcium oxide) has a very high melting point (2$7±
270), it is effective when used as a refractory material, and is particularly stable at high temperatures with low vapor pressure, making it suitable for melting clean metals with few inclusions at high temperatures and reduced pressure. It is.

併しながら石灰質耐火材は、従来からセメント用ロータ
リーキルン、謙導炉、亀弧炉及び硝子炉の内張りの一部
に使用されているに過ぎず、その理由としてはCa○が
水分の存在下で水と反応して水酸化カルシウムを生成し
た保存性が低くなることが挙げられていたのである。
However, calcareous refractory materials have traditionally only been used for part of the lining of cement rotary kilns, Kendo furnaces, Tortoise arc furnaces, and glass furnaces, and the reason for this is that Ca○ is The problem was that it reacted with water to produce calcium hydroxide, which resulted in poor shelf life.

そこでこの欠点を桶なう目的で、従来Ca0に例えばF
e203,Ti02,Si02等の不純物を消化に対す
る安定剤として添加し、耐消化性の石灰質クリンカーを
得ようとすることが行なわれているが斯かる方法では不
純物を添加する工程(各原料の微粉砕工程と混合工程)
に多くの時間と経費がかかり而も工業的に行なわれてい
るように不純物を相当量(5%以上)添加している場合
には添加不純物との間に低融点化合物が生じて耐火性及
び耐貧虫性が劣化すると謂う別途難点が生じたのである
Therefore, in order to overcome this drawback, conventional Ca0, for example, F
Impurities such as e203, Ti02, and Si02 are added as stabilizing agents against digestion in order to obtain a calcareous clinker that is resistant to digestion. process and mixing process)
Although it takes a lot of time and money to add a considerable amount of impurities (5% or more), as is done industrially, a low melting point compound is formed between the added impurities and the fire resistance and Another problem arose when the insect resistance deteriorated.

本発明者達はこれらの事実に鑑み石灰質原料の焼成及び
消化についての実験を繰り返し研究した結果、灼熱減量
測定後の状態でCa0含有量95重量%以上(97.5
重量%以上が望ましい)の高、純度石灰質原料の結晶粒
径が3〜40Aになるように焼成するとFe203,T
i02及びSj02等の不純物を添加しなくても耐消化
性が良好で工業的に充分実用に耐えることを見出し本発
明を完成したのであり、詳しくは石灰質ラミング材の原
料として、灼熱減量測定後の状態がCa○含有量95重
量%以上の石灰石、生石灰又は梢石灰蝦焼物を1600
00以上、好ましくは1600〜180000に加熱し
、その温度で少くとも1.5時間、好ましくは2〜6時
間保持した後、毎時100℃以下の緩慢な率で冷却して
Ca○の結晶粒径が3〜40仏のクリンカ−を得るので
ある。〈なされた石灰質クリンカーは単殊で使用するこ
とができるばかりでなく、これにマグネシアクリンカー
、天然ドロマィトクリンカー又は合成マグネシアドロマ
ィトクリンカーの1種又は2種以上を、混合後の全体量
の45重量%まで添加混合したものについても、何れの
場合も密充填が得られるように粒度調整し、これにアル
コール、ポリプデン、アスフアルト、ピッチ、ワックス
、/ぐラフイン、ポリプロピレン、変性アクリル樹脂、
フェノール樹脂、コールタール及びクマ。ン樹脂等の公
知の非水溶性の有機質結合剤を添加し、ゥェッドパンミ
キサー等の混練機を使用し、加熱鷹練又は常温混練する
ことにより耐消化性及び耐蝕性に優れた石灰質ラミング
材を得るのである。ここにおいて、Ca○の含有量を灼
熱減量後の状態で95重量%以上(97.5重量%程度
のものが望ましい)とする理由は、95重量%未満であ
ると粒子間に多くのガラス層が生成され密封気孔が増加
してラミング材としての機械的強度が小となり耐蝕性、
耐スポール性を低下せしめるのであり、更にCa○の結
晶粒径を3〜40仏とするのは、3仏未満であると水分
との反応性が高まり耐消化性が低下し、40仏を超すと
耐火物として使用中に熱の影響でスポーリングを起し易
くなるからである。
In view of these facts, the present inventors repeatedly conducted experiments on calcining and digestion of calcareous raw materials, and found that the Ca0 content was 95% by weight or more (97.5%) after ignition loss measurement.
Fe203, T
The present invention was completed by discovering that it has good digestion resistance and can be used industrially without adding impurities such as i02 and Sj02. Limestone, quicklime or treetop lime with a Ca○ content of 95% by weight or more is 1600
00 or more, preferably 1,600 to 180,000, and held at that temperature for at least 1.5 hours, preferably 2 to 6 hours, and then cooled at a slow rate of 100 degrees Celsius or less per hour to determine the crystal grain size of Ca○. This means that 3 to 40 Buddhas of clinker can be obtained. <The produced calcareous clinker can not only be used alone, but also one or more types of magnesia clinker, natural dolomite clinker, or synthetic magnesia dolomite clinker can be added to it in an amount of 45% by weight of the total amount after mixing. %, the particle size is adjusted so that close packing can be obtained in each case, and alcohol, polypden, asphalt, pitch, wax, /grafine, polypropylene, modified acrylic resin,
Phenolic resin, coal tar and bears. By adding a known water-insoluble organic binder such as a water-insoluble organic binder, and kneading it under heating or at room temperature using a kneading machine such as a wet pan mixer, a calcareous material with excellent digestibility and corrosion resistance is produced. The ramming material is obtained. Here, the reason why the content of Ca○ is set to be 95% by weight or more (preferably about 97.5% by weight) after ignition loss is that if it is less than 95% by weight, many glass layers will form between the particles. is generated, the number of sealed pores increases, the mechanical strength of the ramming material decreases, and the corrosion resistance increases.
Furthermore, the reason why the crystal grain size of Ca○ should be 3 to 40 degrees is because if it is less than 3 degrees, the reactivity with moisture increases and the digestibility decreases, and if it exceeds 40 degrees, it will reduce the spall resistance. This is because spalling is likely to occur due to the influence of heat during use as a refractory.

又、石灰質クリンカ−に、マグネシアクリンカー、天然
ドロマィトクリンカ−及び合成マグネシアドロマィトク
リンカーの1種又は2種以上を混合する場合の限度を4
5重量%以下とするのは、該量迄の添加においては特に
耐蝕性及び耐スポール性を向上させるが、それ以上添加
すると耐スポール性が却って低下し、且つ石灰質クリン
カーの有する特性が発揮できなくなるからである。以下
本発明の石灰質ラミング材を在来品と比較試験した結果
に就いて詳述すると、石灰質クリンカーとしては第1表
に示す化学組成及び結晶粒径のものを用い、これを第2
表に示す配合割合でそれぞれ調合し、何れも粗粒と紬粒
をウェットパンミキサーに投入し混合した後結合剤を添
加濃練し、その後で徴粉を加えて充分混練するのであっ
て、斯くして得た本発明のラミング材6種類と在来品2
種類とにより、上辺が4伍帆、下辺が6仇舷、高さが5
仇肋の断面台形で長さが100柵のブロックをそれぞれ
2箇宛スタンプ成形して1300ooにて糠成し、それ
らを2箇宛組み合わせて合計16箇回転ドラム内に内張
りセットし、更にスラグと鋼とを7対3の割合でこの中
に入れ】700℃で5時間、所謂、回転侵蝕試験を行い
、溶損寸法を測定した。
In addition, the limit for mixing one or more of magnesia clinker, natural dolomite clinker, and synthetic magnesia dolomite clinker with calcareous clinker has been set to 4.
The reason why the content is 5% by weight or less is that when added up to this amount, corrosion resistance and spalling resistance are particularly improved, but when added more than that, spalling resistance decreases and the properties of calcareous clinker cannot be exhibited. It is from. The results of comparative tests of the calcareous ramming material of the present invention with conventional products will be explained in detail below. Calcareous clinkers having the chemical composition and crystal grain size shown in Table 1 were used, and
After mixing the coarse grains and pongee grains in a wet pan mixer and mixing them, the binder is added and thickened, and then the characteristic powder is added and thoroughly kneaded. 6 types of ramming materials of the present invention and 2 conventional products obtained by
Depending on the type, the upper side is 4 sails, the lower side is 6 sails, and the height is 5 sails.
Two blocks each with a trapezoidal cross section and a length of 100 fences were stamped and brazed at 1,300 oo, then these two blocks were assembled and lined in a total of 16 rotating drums, and then slag and A so-called rotary erosion test was conducted at 700° C. for 5 hours to measure the dimensions of erosion.

又、耐スポーリング性(耐熱衝撃回数)の測定について
は、第1表の化学組成及び結晶粒径のものを用いて第2
表に示す配合割合で得たラミング材を使用して縦5比肋
、横5仇帆、長さ150肋のブロックを各2箇宛成形し
、1300午0にて焼成して供試体とし、これらを電気
炉中へ長さ方向に5仇舷挿入し、1400ooにて15
分間保持した後取出して18分間空冷する。この操作を
供試体の電気炉による、加熱部分が崩壊脱落するまで繰
り返し行った回数を耐熱衝撃回数とし、2箇の平均値で
示す。更に耐消化性は重量増加率により測定し、その方
法は上記と同じラミング材を上蓋のない適当容積の立方
体の容器にそれぞれ充填し、温度25oo、湿度70%
の恒温陣湿槽へ挿入し50日目に取出して水和による重
量増加率を測定した。
In addition, regarding the measurement of spalling resistance (thermal shock resistance number of times), using the chemical composition and crystal grain size shown in Table 1,
Using the ramming material obtained with the compounding ratio shown in the table, two blocks each with a length of 5 ribs, a width of 5 ribs, and a length of 150 ribs were formed, and fired at 1300 o'clock to prepare specimens. Insert these into the electric furnace in the length direction for 5 yards, and at 1400oo
After holding for a minute, it is taken out and air cooled for 18 minutes. The number of times this operation was repeated until the heated part of the test piece collapsed and fell off was defined as the number of times of thermal shock resistance, and the average value of the two values is shown. Furthermore, the digestion resistance is measured by the weight increase rate, and the method is to fill the same ramming material as above into cubic containers of appropriate volume without top lids, and to store them at a temperature of 25 oo and a humidity of 70%.
It was inserted into a constant temperature humidity tank and taken out on the 50th day, and the weight increase rate due to hydration was measured.

以上の結果は、耐蝕性を表わす溶損寸法、と耐消化性を
表す重量増加率及び耐スポーリング性を表わす耐熱衝撃
回数は第2表に示す如く、何れも本発明による供試体N
○、1〜6は明らかに在来品による供試体N○、7〜8
に比して格段の特性向上を示したのである。
The above results show that the erosion dimension, which represents corrosion resistance, the weight increase rate, which represents digestion resistance, and the thermal shock resistance, which represents spalling resistance, are all as shown in Table 2 for the specimen N according to the present invention.
○, 1 to 6 are obviously conventional specimens N○, 7 to 8
It showed a marked improvement in characteristics compared to the previous one.

次に本発明のラミング材の実炉試験として、3屯電気炉
の炉床に均等に張合わせスタンプ施工して従来と同程度
の総精錬屯数である180屯精錬して在来品使用の場合
と比較試験を行なった処、本発明の配合例帆○、1のラ
ミング材の残存厚は、在来品による配合例帆08に比較
して20〜27肋多く、即ち耐蝕性は11〜15%向上
し、同時に消化の兆候は見られず亀裂や剥離現象も殆ん
ど見られないことを確認した。
Next, as an actual furnace test of the ramming material of the present invention, the ramming material was stamped evenly on the hearth of a 3-ton electric furnace, and 180 tons, which is the same total number of smelted tons as in the past, was smelted. Comparison tests were conducted with cases in which the residual thickness of the ramming material for composition example sail ○ and 1 of the present invention was 20 to 27 more than that of composition example sail 08, which was a conventional product, that is, the corrosion resistance was 11 to 1. It was confirmed that there was an improvement of 15%, and at the same time, there were no signs of digestion, and almost no cracking or peeling phenomena were observed.

更に本発明の配合例N○、1とN○、3を同容量の電気
炉の炉床に半張りによるスタンプ施工したところ総精錬
屯数135屯の処理が可能となり、在来品による処理可
能量約10仇歌こ比べ20〜30%増しの良好な結果を
示し、仔細に見ると残存厚はN○、3がN0、1に比較
して5〜15肋多く、耐蝕性の面ではマグネシアを配合
することにより好結果が得られることが証明されたので
ある。
Furthermore, when compounding examples N○, 1 and N○, 3 of the present invention were stamped by half-stretching on the hearth of an electric furnace of the same capacity, it became possible to process a total of 135 tons of refining, which made it possible to process with conventional products. It shows a good result with about 10% more thickness than this, and if you look closely, the residual thickness of N○, 3 is 5 to 15 more than that of N0, 1, and in terms of corrosion resistance, it is superior to magnesia. It has been proven that good results can be obtained by blending.

これらの実炉操業において処理した鋼を切り出し、鋼中
の酸化物系介在物を調べた処、在来品便用による処理鋼
に比較して介在物は少〈石灰質ラミング材から溶鋼中へ
の反応による港出の小さいことも確認されたのである。
When we cut out the steel treated in these actual furnace operations and examined the oxide inclusions in the steel, we found that there were fewer inclusions compared to the steel treated with conventional products. It was also confirmed that the number of ships leaving port due to reactions was small.

叙上の如く本発明は、従来その長所を認められつつも併
存する欠点の為に使用上の限度があった石灰質耐火材に
ついて、その難点を排除して実効性に優れた特性を提供
し、活用範囲を拡大した産業的効果は著しいのである。
第 1 表結晶粒径の測定方法は総べて学振法(耐火物
手張第296〜29刀自、1971年発行)に準じて行
った。
As described above, the present invention eliminates the disadvantages of calcareous refractory materials, which have been recognized for their advantages but had limitations in use due to their accompanying disadvantages, and provides highly effective characteristics. The industrial effects of expanding the range of utilization are significant.
Table 1 All methods for measuring crystal grain sizes were carried out in accordance with the Gakushin method (Refractories Tehari No. 296-29 Toji, published in 1971).

第 2 表(註1)結合剤中のPはボリブテン、Wはワ
ックスを示し添加量は外掛である。
Table 2 (Note 1) In the binder, P represents polybutene and W represents wax, and the amounts added are indicative.

Claims (1)

【特許請求の範囲】 1 CaO含有量が95重量%以上で、且つその結晶粒
径が3〜40μとなるように強焼した後粒度調整した石
灰質クリンカーに、非水溶性の有機質結合剤を添加し、
混合混練して得られる石灰質ラミング材。 2 CaO含有量が95重量%以上で、且つその結晶粒
径が3〜40μとなるように強焼した石灰質クリンカー
と、その45重量%以下の、マグネシアクリンカー、天
然ドロマイトクリンカー、合成マグネシアドロマイトク
リンカーの1種又は2種以上とを混合した後粒度調整し
た配合調整物に、非水溶性の有機質結合剤を添加し、混
合混練して得られる石灰質ラミング材。
[Claims] 1. A water-insoluble organic binder is added to a calcareous clinker that has been hard-fired and adjusted in grain size so that the CaO content is 95% by weight or more and the crystal grain size is 3 to 40μ. death,
Calcareous ramming material obtained by mixing and kneading. 2 Calcareous clinker with a CaO content of 95% by weight or more and a crystal grain size of 3 to 40μ, and 45% by weight or less of magnesia clinker, natural dolomite clinker, synthetic magnesia dolomite clinker. A calcareous ramming material obtained by adding a water-insoluble organic binder to a blended product whose particle size has been adjusted after mixing one type or two or more types, and then mixing and kneading the mixture.
JP51050235A 1976-04-30 1976-04-30 calcareous ramming material Expired JPS6034512B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP51050235A JPS6034512B2 (en) 1976-04-30 1976-04-30 calcareous ramming material

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP51050235A JPS6034512B2 (en) 1976-04-30 1976-04-30 calcareous ramming material

Publications (2)

Publication Number Publication Date
JPS52133310A JPS52133310A (en) 1977-11-08
JPS6034512B2 true JPS6034512B2 (en) 1985-08-09

Family

ID=12853339

Family Applications (1)

Application Number Title Priority Date Filing Date
JP51050235A Expired JPS6034512B2 (en) 1976-04-30 1976-04-30 calcareous ramming material

Country Status (1)

Country Link
JP (1) JPS6034512B2 (en)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS6045245B2 (en) * 1980-11-05 1985-10-08 日立金属株式会社 Method for refining molten metal

Also Published As

Publication number Publication date
JPS52133310A (en) 1977-11-08

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